eudamed_udi
Primary ID: 03760373060038
NashTest (UDI 03760373060038)
Manufactured by Biopredictive
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NashTest - Primary ID 03760373060038
Device Regulatory Overview
The NashTest (Model/Catalog Number: NashTest) is a medical device manufactured by Biopredictive. This product is indexed under FDA Product Code / Category Classification W05030599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NashTest
- Product Code / EMDN
- W05030599
- Device Name
- NashTest
- Database Sync Date
- 2026-08-09 16:48:05
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of NashTest?
The registered manufacturer of record for NashTest is Biopredictive.
What is the Primary UDI-DI identifier for NashTest?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760373060038.
What classification code is assigned to this device?
This device is registered under product classification code W05030599.
Similar Classification Devices (W05030599)
Other Devices by Biopredictive
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